We report here the strategy used in our research group to find a new class of histone deacetylase (HDAC) inhibitors. A series of N-substituted 4-alkylpiperazine and 4- alkylpiperidine hydroxamic acids, corresponding to the basic structure of HDAC inhibitors ...
[Tan, Ping-Zhong; Baldwin, Ronald M.; Fu, Tao; Charney, Dennis S.; Innis, Robert B. Journal of Labelled Compounds and Radiopharmaceuticals, 1999 , vol. 42, # 5 p. 457 - 467]